Canonical Allele Identifier: CA2448298179
Gene: GLA HGNC NCBI
RPL36A-HNRNPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.101398847A= , CM000685.2:g.101398847A= GRCh38
NC_000023.10:g.100653835A= , CM000685.1:g.100653835A= GRCh37
NC_000023.9:g.100540491A= NCBI36
NG_007119.1:g.14117T= , LRG_672:g.14117T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486121.7:c.*185T= (GLA) ENSP00000501124.2:n.*185T=
ENST00000674127.2:c.*242T= (GLA) ENSP00000501044.2:n.*242T=
ENST00000710365.1:c.814T= (GLA) ENSP00000518234.1:p.Ser272=
ENST00000218516.4:c.739T= (GLA) MANE Select ENSP00000218516.4:p.Ser247=
ENST00000466414.2:n.658T= (GLA)
ENST00000468823.2:n.1674T= (GLA)
ENST00000479445.2:n.1136T= (GLA)
ENST00000480513.6:c.*47T= (GLA) ENSP00000497055.1:n.*47T=
ENST00000486121.6:c.784T= (GLA)
ENST00000649178.1:c.862T= (GLA) ENSP00000498186.1:p.Ser288=
ENST00000674127.1:c.839T= (GLA) ENSP00000501044.1:n.839T=
ENST00000674142.1:n.826T= (GLA)
ENST00000674634.2:c.739T= (GLA) ENSP00000502629.2:p.Ser247=
ENST00000675592.1:c.739T= (GLA) ENSP00000502239.1:p.Ser247=
ENST00000675799.1:c.*47T= (GLA) ENSP00000502661.1:n.*47T=
ENST00000675968.1:n.3393T= (GLA)
ENST00000676156.1:c.703T= (GLA) ENSP00000501730.1:p.Ser235=
ENST00000676372.1:c.739T= (GLA) ENSP00000502805.1:p.Ser247=
ENST00000218516.3:c.739T= (GLA) ENSP00000218516.3:p.Ser247=
ENST00000409170.3:c.300+3390A= (RPL36A-HNRNPH2) ENSP00000386655.4:n.300+3390A=
ENST00000409338.5:c.177+7025A= (RPL36A-HNRNPH2) ENSP00000386974.2:n.177+7025A=
ENST00000468823.1:n.288T= (GLA)
ENST00000480513.5:n.577T= (GLA)
ENST00000493905.6:c.*127T= (GLA) ENSP00000476935.1:n.*127T=
NM_000169.2:c.739T= , LRG_672t1:c.739T= (GLA) NP_000160.1:p.Ser247=
NM_001199973.1:c.408+3390A= (RPL36A-HNRNPH2) NP_001186902.1:n.408+3390A=
NM_001199974.1:c.285+7025A= (RPL36A-HNRNPH2) NP_001186903.1:n.285+7025A=
XR_938397.1:n.824T= (GLA)
XR_938397.2:n.845T= (GLA)
NM_001199973.2:c.300+3390A= (RPL36A-HNRNPH2) NP_001186902.2:n.300+3390A=
NM_001199974.2:c.177+7025A= (RPL36A-HNRNPH2) NP_001186903.2:n.177+7025A=
NM_000169.3:c.739T= (GLA) MANE Select NP_000160.1:p.Ser247=
NR_164783.1:n.818T= (GLA)